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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1784044Generated: October 29, 2026

Hydrochloric Acid → HCID 66880761, compound

https://huagongshe.com/reaction/1784044

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantLithium HexamethyldisilazideHCID 2733832—
ReactantEthyl 3-(4-chlorophenyl)-2,4-dioxo-3-azabicyclo[3.1.0]hexane-6-carboxylateHCID 3120146—
Reactant1-(4-Amino-3-fluorophenyl)pyridin-2-oneHCID 22181548—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66880761HCID 6688076124%

Reaction Steps

A solution of 7 g (34 mmol) of 1-(4-amino-3-fluoro-phenyl)-1H-pyridin-2-one (prepared according to C. F. Bigge et al., patent application WO 2003045912) in 25 ml of THF was cooled to −78° C. and treated dropwise with 41 ml of a 1M lithium bis(trimethylsilyl)amide-solution in THF and stirred for 30 min. To this solution 9.5 g (32 mmol) of (1RS, 5SR, 6R)-3-(4-chloro-phenyl)-2,4-dioxo-3-aza-bicyclo[3.1.0]hexane-6-carboxylic acid ethyl ester were added portionwise and the mixture was allowed to reach room temperature within a few hours. The mixture was then poured into a diluted aqueous HCl-solution (ca. 0.2 M) and extracted with AcOEt. The combined organic phases were dried with Na2SO4. Evaporation of the solvent and chromatography on silica gel with dichloromethane and then with a gradient of dichloromethane/MeOH from 98:2 to 95:5 gave 4.1 g (24%) of the title compound. Light brown solid. MS: 496 (M−H)−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07501413B2
Source datasetuspto-grants-2009_03
ORD IDord-f0500249342f437da4972a50b3c26b60
Source noteuspto-grants-2009_03